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Discussion papers
https://doi.org/10.5194/acp-2019-395
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-2019-395
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.

Submitted as: research article 17 May 2019

Submitted as: research article | 17 May 2019

Review status
This discussion paper is a preprint. A revision of this manuscript was accepted for the journal Atmospheric Chemistry and Physics (ACP) and is expected to appear here in due course.

Effect of NOx on 1,3,5-trimethylbenzene (TMB) oxidation product distribution and particle formation

Julia Hammes1, Epameinondas Tsiligiannis1, Thomas F. Mentel1,2, and Mattias Hallquist1 Julia Hammes et al.
  • 1Department of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg, Sweden
  • 2Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, Jülich, Germany

Abstract. Secondary organic aerosol (SOA) represents a significant fraction of the tropospheric aerosol and its precursors are volatile organic compounds (VOC). Anthropogenic VOCs (AVOC) dominate the VOC budget in many urban areas with 1,3,5-trimethylbenzene (TMB) being among the most reactive aromatic AVOCs. TMB formed highly oxygenated organic molecules (HOM) in NOx free environment, which could contribute to new particle formation (NPF) depending on oxidation conditions were elevated OH oxidation enhanced particle formation. The experiments were performed in an oxidation flow reactor, the Go : PAM unit, under controlled OH oxidation conditions. By addition of NOx to the system we investigated the effect of NOx on particle formation and on the product distribution. We show that the formation of HOM and especially HOM accretion products, strongly varies with NOx conditions. We observe a suppression of HOM and particle formation with increasing NOx / ΔTMB and an increase in the formation of organonitrates (ON) mostly at the expense of HOM accretion products. We propose reaction mechanisms/pathways that explain the formation and observed product distributions with respect to oxidation conditions. We hypothesize that, based on our findings from TMB oxidation studies, aromatic AVOCs may not contribute significantly to NPF under typical NOx / AVOC conditions found in urban atmospheres.

Julia Hammes et al.
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AC: Author comment | RC: Referee comment | SC: Short comment | EC: Editor comment
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Interactive discussion
Status: closed
Status: closed
AC: Author comment | RC: Referee comment | SC: Short comment | EC: Editor comment
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Julia Hammes et al.
Julia Hammes et al.
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